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Last Updated: December 28, 2025

Claims for Patent: 10,105,418


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Summary for Patent: 10,105,418
Title:Oral administration of tocilizumab treatment of autoimmune disease
Abstract: The present invention provides a method for treating or delaying the onset of an autoimmune condition in a human subject comprising orally administering to the subject at an effective dose of tocilizumab.
Inventor(s): Brod; Staley A. (Bellaire, TX)
Assignee:
Application Number:14/139,122
Patent Claims:1. A method for treating or delaying the onset of an autoimmune condition in a human subject comprising orally administering tocilizumab to the subject; wherein said autoimmune condition is multiple sclerosis or rheumatoid arthritis.

2. The method of claim 1, wherein the tocilizumab is administered in a liquid form.

3. The method of claim 1, wherein the tocilizumab is administered in a solid form.

4. The method of claim 1, wherein tocilizumab is administered in a dose from 1.0 .mu.g to 50 .mu.g.

5. The method of claim 4, wherein tocilizumab is administered in a dose from 1 .mu.g to 10 .mu.g.

6. The method of claim 1, wherein said tocilizumab administration decreases levels of IL-6, Th1-like cytokines IL-2, IL-12, TNF-.alpha. and IFN-.gamma..

7. The method of claim 1, wherein said tocilizumab administration increases levels of IL-4, IL-10 and IL-13.

8. The method of claim 1, further comprising administering a compound selected from the group consisting of a SIRS peptide, .alpha.-MSH, ACTH and SST.

9. A method for decreasing innate inflammatory cytokines IL-1.beta. and TNF-.alpha., Th1-like cytokines IL-2 and IFN-.gamma., IL-17 (T.sub.eff), IL-12p70 and increasing the Th2-like counter-regulatory cytokine IL-13 in a human subject comprising orally administering tocilizumab to the subject.

10. The method of claim 9, wherein the tocilizumab is administered in a liquid form.

11. The method of claim 9, wherein tocilizumab is administered in a solid form.

12. The method of claim 9, wherein tocilizumab is administered in a dose from 1.0 .mu.g to 50 .mu.g.

13. The method of claim 12, wherein tocilizumab is administered in a dose from 1 .mu.g to 10 .mu.g.

14. The method of claim 9, further comprising administering a compound selected from the group consisting of a SIRS peptide, .alpha.-MSH, ACTH and SST.

Details for Patent 10,105,418

Applicant Tradename Biologic Ingredient Dosage Form BLA Approval Date Patent No. Expiredate
Genentech, Inc. ACTEMRA tocilizumab Injection 125276 January 08, 2010 10,105,418 2033-12-23
Genentech, Inc. ACTEMRA tocilizumab Injection 125472 October 21, 2013 10,105,418 2033-12-23
Genentech, Inc. ACTEMRA tocilizumab Injection 125472 November 19, 2018 10,105,418 2033-12-23
>Applicant >Tradename >Biologic Ingredient >Dosage Form >BLA >Approval Date >Patent No. >Expiredate

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